University of California-Riverside, Department of Chemistry, Riverside, CA, 92521, USA.
University of California-Riverside, Environmental Toxicology Program, Riverside, CA, 92521, USA.
Angew Chem Int Ed Engl. 2018 Nov 26;57(48):15675-15680. doi: 10.1002/anie.201806901. Epub 2018 Oct 30.
Extracellular vesicles (EVs) actively participate in intercellular communication and pathological processes. Studying the molecular signatures of EVs is key to reveal their biological functions and clinical values, which, however, is greatly hindered by their sub-100 nm dimensions, the low quantities of biomolecules each EV carries, and the large population heterogeneity. Now, single-EV flow cytometry analysis is introduced to realize single EV counting and phenotyping in a conventional flow cytometer for the first time, enabled by target-initiated engineering (TIE) of DNA nanostructures on each EV. By illuminating multiple markers on single EVs, statistically significant differences are revealed among the molecular signatures of EVs originating from several breast cancer cell lines, and the cancer cell-derived EVs among the heterogeneous EV populations are successfully recognized. Thus, our approach holds great potential for various biological and biomedical applications.
细胞外囊泡(EVs)积极参与细胞间通讯和病理过程。研究 EV 的分子特征对于揭示其生物学功能和临床价值至关重要,但 EV 的亚 100nm 尺寸、每个 EV 携带的生物分子数量少以及群体异质性大极大地阻碍了这一进程。现在,通过在每个 EV 上进行目标起始工程(TIE)的 DNA 纳米结构,首次实现了在传统流式细胞仪中对单个 EV 进行计数和表型分析。通过对单个 EV 上的多个标记物进行检测,揭示了来自几种乳腺癌细胞系的 EV 之间的分子特征存在显著差异,并且能够成功识别异质 EV 群体中的癌细胞衍生 EV。因此,我们的方法在各种生物学和生物医学应用中具有很大的潜力。